FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SCHIFF REAGENT

K Number: K883217 · Decision Aug 5, 1988
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
4
Applicant Total
30
Review Days
7

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Basic Information

Device Name
SCHIFF REAGENT
K Number
K883217
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.1850
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Surgipath Medical Industries, Inc.
Date Received
July 29, 1988
Decision Date
August 5, 1988
Product Code
HZT
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HZT Reagent, Schiff

Similar 510(k) Clearances

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Other Clearances by Surgipath Medical Industries, Inc.

K Number Device Name
K881921 C-E BRUSH
K881922 CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE
K881659 TISSUE SECTION ADHESIVE
K863549 REUSABLE/DISPOSABLE AUTOPSY KNIFE SET
K863616 KNIFE MAKER
K863548 ROTARY MICROTOME
K863483 CASSETTE EMBOSSEER
K863145 CERVICAL SCRAPERS
K861270 BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.
K861201 FORMALDEHYDE SOLUTION, 37%
Search all 30 clearances from Surgipath Medical Industries, Inc. →